Palvella Therapeutics, Inc. (PVLA) Documents: SEC Filings, Investor Presentations & Press Releases

Palvella Therapeutics, Inc. (PVLA) documents, SEC filings and the IR site together: 131 documents, newest first; latest 2026-08-05. Read in-app with summaries. First-party data.

Documents — U.S. SEC EDGAR and the company's IR site
DateTypeDocument
2026-08-05Press releasePalvella Therapeutics to Participate in the Canaccord Genuity 46th Annual Growth Conference
2026-08-04Press releasePalvella Therapeutics Reports Second Quarter 2026 Financial Results and Provides Corporate Update
2026-08-048-KForm 8-K, Item 2.02 results
2026-08-0410-QForm 10-Q for the quarter ended Jun 30
2026-08-04TranscriptQ2 FY26 earnings call transcript
2026-07-30Press releasePalvella Therapeutics Chief Scientific Officer Jeff Martini, Ph.D. Selected to Present at Upcoming FDA Public Workshop o
2026-07-28Press releasePalvella Therapeutics to Host Second Quarter 2026 Financial Results and Corporate Update Conference Call on August 4, 20
2026-07-14DeckFirst-in-disease therapies for patients with rare diseases Corporate Presentation
2026-07-148-KForm 8-K, Item 8.01
2026-06-30Press releasePalvella Therapeutics Appoints Accomplished Rare Disease Biotech Executive and Commercial Leader Matt Pauls, J.D., M.B.A., to Board of Directors
2026-06-308-KForm 8-K, Item 5.02
2026-06-29Press releasePalvella Therapeutics Submits First Module of Rolling New Drug Application to FDA for QTORIN™ Rapamycin for the Treatment of Microcystic Lymphatic Malformations
2026-06-22Press releaseFDA Grants Rolling Review of Palvella’s QTORIN™ Rapamycin NDA for Microcystic Lymphatic Malformations
2026-06-168-KForm 8-K, Item 5.02
2026-06-03Press releasePalvella Therapeutics Announces Completion of FDA Pre-NDA Meeting for QTORIN™ Rapamycin in Microcystic Lymphatic Malformations
2026-06-02Press releasePalvella Therapeutics to Participate in the Goldman Sachs 47th Annual Global Healthcare Conference 2026
2026-05-27Press releasePalvella Therapeutics Strengthens QTORIN™ Pitavastatin Intellectual Property with Yale-Licensed U.S. Patent Providing Protection into 2043
2026-05-20DeckInvestor presentation · May 2026
2026-05-208-KForm 8-K, Item 8.01
2026-05-15Press releasePalvella Therapeutics Announces New Data from the Phase 2 TOIVA Trial of QTORIN™ Rapamycin in Cutaneous Venous Malformations Presented at the 83rd Annual Meeting of the Society for Investigative Dermatology
2026-05-158-KForm 8-K, Item 8.01
2026-05-138-KForm 8-K, Item 8.01
2026-05-078-KForm 8-K, Item 2.02 results
2026-05-0710-QForm 10-Q for the quarter ended Mar 31
2026-05-04Press releasePalvella Therapeutics Announces First Patients Dosed in Phase 2 LOTU Trial of Fast Track-Designated QTORIN™ Rapamycin for Clinically Significant Angiokeratomas
2026-04-30ProxyDefinitive proxy statement
2026-04-20Press releasePalvella Therapeutics to Present QTORIN™ Rapamycin Results from Phase 3 SELVA and Phase 2 TOIVA Studies at the International Society for the Study of Vascular Anomalies World Congress 2026
2026-04-138-KForm 8-K, Item 5.02
2026-04-078-KForm 8-K, Item 8.01
2026-03-31Press releasePalvella Therapeutics Reports Full Year 2025 Financial Results and Provides Corporate Update
2026-03-318-KForm 8-K, Item 2.02 results
2026-03-3110-KAnnual report on Form 10-K, FY25
2026-03-27Press releasePalvella Therapeutics Highlights Continued Progress Across Rare Skin Disease Pipeline with Two Poster Presentations at the 2026 American Academy of Dermatology Annual Meeting
2026-03-24Press releasePalvella Therapeutics to Host Full Year 2025 Financial Results Conference Call and Provide a Corporate Update on March 31, 2026
2026-02-268-KForm 8-K, Item 1.01
2026-02-24DeckFirst-in-disease therapies for patients with rare diseases Phase 3 SELVA Topline Data in Microcystic Lymphatic Malformations · Q1 2026
2026-02-24Press releasePalvella Therapeutics Announces Positive Topline Results from Phase 3 SELVA Clinical Study of QTORIN™ 3.9% Rapamycin Anhydrous Gel (QTORIN™ rapamycin) in Microcystic Lymphatic Malformations
2026-02-248-KForm 8-K, Item 8.01
2026-02-248-KForm 8-K, Item 7.01
2026-02-248-KForm 8-K, Item 2.02 results

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Data sourced from U.S. SEC EDGAR and the company's investor-relations site. Not personalized investment advice.